3,6,9,12-Tetraoxatetracosanoic acid

Base Information

Chemical Name:3,6,9,12-Tetraoxatetracosanoic acid
CAS No.:20858-25-7
Molecular Formula:C₂₀H₄₀O₆
Molecular Weight:376.534
Hs Code.:
DSSTox Substance ID:DTXSID70943112
Wikidata:Q82920159
Mol file:20858-25-7.mol

Synonyms:3,6,9,12-Tetraoxatetracosanoic acid;20858-25-7;2-[2-[2-(2-dodecoxyethoxy)ethoxy]ethoxy]acetic acid;SCHEMBL10039252;DTXSID70943112;3,6,9,12-Tetraoxatetracosan-1-oic acid;NS00095094

Suppliers and Price of 3,6,9,12-Tetraoxatetracosanoic acid

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 4 raw suppliers

Chemical Property of 3,6,9,12-Tetraoxatetracosanoic acid

Chemical Property:

PSA：74.22000
LogP:4.05830
XLogP3:4.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:22
Exact Mass:376.28248899
Heavy Atom Count:26
Complexity:286

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCCCOCCOCCOCCOCC(=O)O

Technology Process of 3,6,9,12-Tetraoxatetracosanoic acid

There total 3 articles about 3,6,9,12-Tetraoxatetracosanoic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 62.0%

: 3055-94-5,9015-55-8
2-[2-(2-Dodecyloxy-ethoxy)-ethoxy]-ethanol

: 3926-62-3
sodium monochloroacetic acid

: 20858-25-7,27306-90-7
{2-[2-(2-Dodecyloxy-ethoxy)-ethoxy]-ethoxy}-acetic acid

Guidance literature:: With sodium; In xylene; at 110 - 130 ℃; for 16h;

Reference yield:

: 5274-68-0,9015-55-8
tetraethylene glycol monododecyl ether

: 20858-25-7,27306-90-7
{2-[2-(2-Dodecyloxy-ethoxy)-ethoxy]-ethoxy}-acetic acid

Guidance literature:: With Jones reagent; In acetone; at 20 ℃;
DOI:10.1002/rcm.4624

Reference yield:

: 112-53-8
1-dodecyl alcohol

: 20858-25-7,27306-90-7
{2-[2-(2-Dodecyloxy-ethoxy)-ethoxy]-ethoxy}-acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: sodium hydroxide / 4.5 h / 105 °C / Inert atmosphere

2: sodium hypochlorite / 1.5 h / 125 °C

With sodium hypochlorite; sodium hydroxide;